Project Manager - Pharmacovigilience

Investigo; London; Hybrid; GBP 65,000 - 85,000; Full time

Job summary

A leading pharmaceutical brand is seeking a PV Senior Project Manager to join their team in London. The role involves significant project management responsibilities in pharmacovigilance and requires strong leadership skills and client-facing experience. Ideal candidates will have 8+ years in project management within the life sciences sector, ensuring successful client software implementations while adhering to industry regulations.

Qualifications

• 8+ years of experience in project management, with at least 5 years in a senior or lead role.
• Proven experience managing pharmacovigilance, clinical, or regulatory technology projects.

Responsibilities

• Lead end-to-end project management of client software implementations, upgrades, and integrations.
• Coordinate cross-functional, global teams to ensure successful project delivery.
• Develop and manage project plans, including timelines, budgets, and resource demands.

Skills

Project Management

Client Relationship Management

Leadership

Risk Management

Pharmacovigilance Knowledge

Education

Bachelor's or Master's degree in Computer Science, Information Technology, Project Management

Tools

Agile

Scrum

Waterfall

Job description

PV Senior Project Manager

London / Remote / Hybrid

Leading Pharmaceutical Brand is seeking to hire an established Project Manager with strong pharmacovigilance project delivery experience to join their expanding centralised senior team.

The ideal candidate will be a dynamic client facing services professional with extensive project management experience in the life science technology domain. This is a strategic role requiring deep project management expertise, pharmaceutical domain knowledge, and excellent leadership skills.

Key Responsibilities:

Lead end-to-end project management of client software implementations, upgrades, and integration's.

Develop and manage project plans, including time-lines, budgets, and resource demand, and author project initiation documents.

Coordinate cross-functional, global teams to ensure successful project delivery.

Serve as the primary point of contact for senior client stakeholders, ensuring clear communication and strong relationship management.

Ensure the accuracy, reliability, and performance of all project deliverable.

Monitor project progress and performance, identifying and mitigating risks and issues as they arise.

Facilitate regular project status meetings and provide updates to stakeholders.

Actively manage project scope and costs, ensuring any changes are documented and approved through formal change control processes.

Develop and maintain comprehensive project documentation, including project initiation documents, risk management plans, and post-project reviews.

Ensure all projects comply with industry regulations, particularly those related to pharmacovigilance and data privacy (e.g. GxP, GDPR).

Selection criteria

PV Client facing system implementation experience essential. (PV, GxP, GAMP4/5)

Bachelor's or Master's degree in Computer Science, Information Technology, Project Management, or a related field.

8+ years of experience in project management, with at least 5 years in a senior or lead role delivering software solutions to pharmaceutical or life sciences clients.

Proven experience managing pharmacovigilance, clinical, or regulatory technology projects.

Knowledge of pharmacovigilance workflows and regulatory standards

Expertise in project management methodologies (e.g., Agile, Scrum, Waterfall).

Interested in being considered? Apply to Investigo without delay.